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NeoLIPA: Neoadjuvant LTX-315 in Combination with Pembrolizumab in Resectable Stage III/IV Melanoma

Study acronym: NeoLIPA
StatusRecruiting
PhasePhase 2
Started2024-11-01
View on ClinicalTrials.gov ↗
Record status
This record was last updated October 26, 2024 (before its estimated May 2026 completion). Its status may not reflect the trial's current state.

Amendment history

2024-10-23
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Study sitesdetails revised at 1 of 1 site
2024-10-20
minor
Study Identification, Study Status, Sponsor/Collaborators, Contacts/Locations v1
Study sitesdetails revised at 1 of 1 site
Study titlerevised
NeoLIPA: Neoadjuvant LTX-315 in Combination Withwith Pembrolizumab in Resectable Stage III/IV Melanoma
2024-10-18
minor
Original filing
1,020 trials monitored
See 45 trials at risk
This clinical trial aims to evaluate the effectiveness of a new treatment approach for patients with stage III or IV melanoma that has spread to other parts of the body but can still be surgically removed. The study combines two treatments: LTX-315 and pembrolizumab. Melanoma that has spread to other parts of the body can often be treated with surgery. Despite surgery, there is a high risk of the cancer coming back. Pembrolizumab, an immune checkpoint inhibitor, can reduce this risk when given after surgery. Recent studies have shown that giving pembrolizumab before surgery, along with post-surgery treatment, might be more effective than giving it only after surgery. However, many patients still experience cancer recurrence. Combining pembrolizumab with LTX-315, which triggers a different immune response, might improve the treatment\'s effectiveness and reduce the risk of cancer progression before surgery. This is an open-label Phase II study, meaning both the researchers and participants will know which treatments are being given. The study will be conducted at a single center and will involve about 27 participants. They will receive LTX-315 and pembrolizumab before their planned surgery to see if this combination could be more effective than pembrolizumab alone. The primary goal is to assess the tumors response to the neoadjuvant (pre-surgery) treatment, specifically looking at the rate of pathological complete response (pCR), where no cancer is detected in the removed tumor tissue.
Trial Details
NCT Number NCT06651151
Lead Sponsor Oslo University Hospital
Collaborators: Lytix Biopharma AS
Conditions Melanoma Stage IIIB-IV
Enrollment 27 participants
Start Date 2024-11-01
Primary Completion 2026-05 (estimated)
Study Completion 2031-05 (estimated)
Updated on ClinicalTrials.gov 2024-10-26